LBF16000HO03: Difference between revisions

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|LipidMaps=LMFA01050049
|LipidMaps=LMFA01050049
|SysName=11-Hydroxyhexadecanoic acid
|SysName=11-Hydroxyhexadecanoic acid
|Common Name=&&11-Hydroxypalmitic acid&&builic acid&&jalapinoic acid&&11-Hydroxyhexadecanoic acid&&
|Common Name=&&11-Hydroxypalmitic acid&&Builic acid&&Jalapinoic acid&&
|Melting Point=68-69°C
|Melting Point=68-69°C
|Boiling Point=183-186°C at 3 mm Hg
|Boiling Point=183-186°C at 3 mm Hg
|Solubility=soluble in ethyl alcohol and ether[[Reference:Davies_LA:Gardner_WH:,J. Am. Chem. Soc.,1942,,|{{RelationTable/GetFirstAuthor|Reference:Davies_LA:Gardner_WH:,J. Am. Chem. Soc.,1942,,}}]][[Reference:Sen_Gupta_R:Bose_PK:,J. Sci. Ind. Res.,1952,11,458|{{RelationTable/GetFirstAuthor|Reference:Sen_Gupta_R:Bose_PK:,J. Sci. Ind. Res.,1952,11,458}}]]
|Solubility=soluble in ethyl alcohol and ether[[Reference:Davies_LA:Gardner_WH:,J. Am. Chem. Soc.,1942,,|{{RelationTable/GetFirstAuthor|Reference:Davies_LA:Gardner_WH:,J. Am. Chem. Soc.,1942,,}}]]<!--0263-->[[Reference:Sen_Gupta_R:Bose_PK:,J. Sci. Ind. Res.,1952,11,458|{{RelationTable/GetFirstAuthor|Reference:Sen_Gupta_R:Bose_PK:,J. Sci. Ind. Res.,1952,11,458}}]]
|Source=Shellac; root wax of Ipomoea orizabensis (Mexican scammony)
|Chemical Synthesis=
|Metabolism=
}}
}}


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Latest revision as of 06:00, 15 April 2010

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Upper classes: LB LBF



11-Hydroxypalmitic acid
Structural Information
11-Hydroxyhexadecanoic acid
  • 11-Hydroxypalmitic acid
  • Builic acid
  • Jalapinoic acid
Formula C16H32O3
Exact Mass 272.23514489
Average Mass 272.42348
SMILES CCCCCC(O)CCCCCCCCCC(O)=O
Physicochemical Information
68-69°C
183-186°C at 3 mm Hg
soluble in ethyl alcohol and ether Davies_LA et al. Sen_GuptaRet al.
Shellac; root wax of Ipomoea orizabensis (Mexican scammony)
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
[hide]Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF16000HO03 See above. Davies_LA et al. 1942
n.a. LBF16000HO03 See above. Sen_Gupta_R et al. 1952